The human germ cell-less (HGCL): A candidate gene for Alström syndrome

Keyphrases

• Human Germ Cells 100%
• Germ Cell-less 100%
• Deafness 20%
• Expression Pattern 20%
• Associated Functions 20%
• Linkage Analysis 20%
• Transcriptional Activity 20%
• Obesity 20%
• Human Tissue 20%
• Autosomal Recessive 20%
• Transcriptional Repression 20%
• Hepatic Dysfunction 20%
• Chromosomal Region 20%
• Drosophilidae 20%
• Retinitis pigmentosa 20%
• Cardiomyopathy 20%
• Regulatory Proteins 20%
• Human Homolog 20%
• Negatively Regulate 20%
• Non-insulin-dependent Diabetes Mellitus (NIDDM) 20%
• POZ Domain 20%
• ALMS1 20%
• DCTN1 20%
• Chromosomal Mapping 20%
• Chronic Progressive Nephropathy 20%
• Male Hypogonadism 20%
• Acanthosis Nigricans 20%

Biochemistry, Genetics and Molecular Biology

• Candidate Gene 100%
• Mouse 66%
• Transcription 33%
• Linkage Analysis 33%
• Autosomal Recessive Disorder 33%
• ALMS1 33%
• DCTN1 33%
• Hyperlipidemia 33%
• BTB/POZ Domain 33%
• Cell Cycle 33%
• E2F 33%
• Chromosomal Mapping 33%
• Retinitis pigmentosa 33%